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Resolution of the Vertical and Horizontal Heterogeneity of Adsorbed Collagen Layers by Combination of QCM-D and AFM

Year: 2005

Journal: Langmuir 2005, 21, 10684-10692, 20100827

Authors: Gurdak E., Dupont-Gillain C.C, Booth J., Roberts C.J., Rouxhet P.G

Last authors: Paul G. Rouxhet

Organizations: Unité de Chimie des Interfaces, Université Catholique de Louvain, Croix du Sud 2/18, 1348 Louvain-la-Neuve, Belgium, Scientific & Medical Products Ltd., Shirley House, 12 Gatley Road, Cheadle Cheshire, SK8 1PY United Kingdom, and Laboratory of Biophysics and Surface Analysis, School of Pharmacy, The University of Nottingham, Nottingham, NG7 2RD United Kingdom

Country: UK, United Kingdom

Collagen (type I from calf skin) adsorption on polystyrene (PS) and plasma-oxidized polystyrene (PSox) was studied, using a quartz crystal microbalance with energy dissipation measurements (QCM-D) and atomic force microscopy (AFM) in tapping mode. Radio-labeled collagen was used to measure the adsorbed amount and the ability of adsorbed collagen to exchange with molecules in the solution. The results show that the collagen adlayer consists of two parts: a dense and thin sheet in which fibrils are formed (directly observed by AFM) and an overlying thick layer (up to 200 nm) containing protruding molecules or bundles which are in very low concentration but modify noticeably the local viscosity. The thickness and viscosity of the semi-liquid adlayer both increase with adsorption time and collagen concentration. Fibril formation near the surface also increases with time and collagen concentration and occurs more readily on PS compared to PSox. Radiochemical measurements show that this may be related to the larger mobility of molecules adsorbed on PS, presumably owing to a smaller number of binding points.